Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
99051 BAA10g06360 A10 3269938 C T missense_variant MODERATE c.1661G>A|p.Arg554Lys S281
99052 BAA10g06370 A10 3270184 C T upstream_gene_variant MODIFIER c.-3588C>T| S23
99053 BAA10g06360 A10 3270407 G A missense_variant MODERATE c.1379C>T|p.Ser460Phe S69
99054 BAA10g06360 A10 3270730 G A synonymous_variant LOW c.1149C>T|p.Ile383Ile S302
99055 BAA10g06370 A10 3271045 C T upstream_gene_variant MODIFIER c.-2727C>T| S122
99056 BAA10g06360 A10 3271331 G A missense_variant MODERATE c.799C>T|p.Leu267Phe S295
99057 BAA10g06360 A10 3271895 C T missense_variant MODERATE c.316G>A|p.Glu106Lys S68
99058 BAA10g06360 A10 3272606 G A upstream_gene_variant MODIFIER c.-292C>T| S292
99059 BAA10g06360 A10 3272974 G A upstream_gene_variant MODIFIER c.-660C>T| S192
99060 BAA10g06360 A10 3273502 C T upstream_gene_variant MODIFIER c.-1188G>A| S15
S156
S2
S3
S34
99061 BAA10g06360 A10 3273916 C T upstream_gene_variant MODIFIER c.-1602G>A| S270
99062 BAA10g06390 A10 3275645 C T synonymous_variant LOW c.93C>T|p.Ala31Ala S121
99063 BAA10g06360 A10 3276660 G A upstream_gene_variant MODIFIER c.-4346C>T| S32
99064 BAA10g06400 A10 3277316 G A upstream_gene_variant MODIFIER c.-85G>A| S125
99065 BAA10g06400 A10 3277338 C T upstream_gene_variant MODIFIER c.-63C>T| S41
99066 BAA10g06370 A10 3278042 G A downstream_gene_variant MODIFIER c.*3484G>A| S212
99067 BAA10g06380 A10 3279683 G A downstream_gene_variant MODIFIER c.*4149G>A| S217
S248
99068 BAA10g06380 A10 3279945 G A downstream_gene_variant MODIFIER c.*4411G>A| S81
S85
99069 BAA10g06390 A10 3281140 C T downstream_gene_variant MODIFIER c.*4666C>T| S244
99070 BAA10g06390 A10 3281458 C T downstream_gene_variant MODIFIER c.*4984C>T| S116
99071 BAA10g06410 A10 3282296 C T stop_gained HIGH c.1950G>A|p.Trp650* S2
99072 BAA10g06410 A10 3282559 C T splice_region_variant&intron_variant LOW c.1776+3G>A| S44
99073 BAA10g06410 A10 3282788 G A intron_variant MODIFIER c.1694-144C>T| S202
99074 BAA10g06410 A10 3282814 C T intron_variant MODIFIER c.1693+128G>A| S297
99075 BAA10g06420 A10 3283670 G A downstream_gene_variant MODIFIER c.*4718C>T| S283